A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096949



Internal ID22006182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16353365..16353365hg38UCSC Ensembl
chr17:16256679..16256679hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630445
Samples
Known GenesCENPV
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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